Novel copy number variations within SYCE1 caused meiotic arrest and non-obstructive azoospermia

Background Non-obstructive azoospermia (NOA) is the most severe disease in male infertility, but the genetic causes for majority of NOA remain unknown. Methods Two Chinese NOA-affected patients were recruited to identify the genetic causal factor of infertility. Whole-exome sequencing (WES) was conducted in the two patients with NOA. Sanger sequencing and CNV array were used to ascertain the WES results. Hematoxylin and eosin (H&E) staining and immunofluorescence (IF) were carried out to evaluate the stage of spermatogenesis arrested in the affected cases. Results Novel heterozygous deletion (LOH) within SYCE1 (seq[GRCh37] del(10)(10q26.3)chr10:g.135111754_135427143del) and heterozygous loss of function (LoF) variant in SYCE1 (NM_001143763: c.689_690 del:p.F230fs) were identified in one NOA-affected patient. While homozygous deletion within SYCE1 (seq[GRCh37] del(10)(10q26.3)chr10:g.135340247_135379115del) was detected in the other patient with meiotic arrest. H&E and IF staining demonstrated that the spermatogenesis was arrested at pachytene stage in the two patients with NOA, suggesting these two novel CNVs within SYCE1 could lead to meiotic defect and NOA. Conclusions We identified that two novel CNVs within SYCE1 are associated with meiotic arrest and male infertility. Thus, our study expands the knowledge of variants in SYCE1 and provides a new insight to understand the genetic etiologies of NOA. Supplementary Information The online version contains supplementary material available at 10.1186/s12920-022-01288-8.

pathologic analysis, NOA could be classified into three types, including Sertoli cell only syndrome (SCOS), maturation arrest (MA) and hypo-spermatogenesis (HS). MA is characterized by the presence of germ cells that do not complete spermatogenic development, most of which is meiotic arrest. It was showed that complete germ cell arrest occurs at the spermatocyte period in 12% azoospermic men [1].
Genetic etiology has been revealed for meiotic defects in recent decades. It is illustrated that translocation between autosome and sex chromosome was associated with meiotic defects mainly due to the chromosomal pairing disturbances around the breakpoints [2][3][4]. Micro-deletions of Y chromosome could result in meiotic defects mainly because of deficiency in RNA Binding Motif Protein X-Linked (RBMY), the RNA binding protein located in Y chromosome [5][6][7]. Furthermore, through whole-exome sequencing (WES) of NOA pedigree study, several single-nucleotide variants (SNVs) and inDels have been identified as the cause of meiotic defects in human, including DNA Meiotic  [8][9][10][11][12][13][14][15][16]. Recent years have seen the emergence of copy number variation (CNV) as an important source of genetic diversity. CNVs are defined as submicroscopic chromosomal deletions, insertions or duplications in the human genome ranging from 50 bp to several Mb [17]. It is estimated that approximately 5-10% of the human genome contributed to CNVs. Most CNVs are benign, however, maladaptive CNVs are associated with common or rare genetic disorders, such as autism [18], type 1 diabetes [19], Charcot-Marie-Tooth disease type 1A [20], and hemophilia A [21]. CNVs were also associated with meiotic arrest. It is illustrated that eight deletions/duplications might be linked with maturation arrest [22]. Moreover, it is identified that heterozygous duplication in MAST2, MYRIP, LRRC4C and the long noncoding RNA LOC100507205 are associated with meiotic arrest [23,24]. However, the roles of MAST2, MYRIP, LRRC4C and the long noncoding RNA LOC100507205 were unknown in the germ cell development. It was illustrated that a homozygous deletion of the entire open reading frame of the SYCE1 gene has been reported in a sporadic NOA patient [25]. Also, Huang et al. identified one homozygous CNV within 134-kb deletion on chromosome 10 encompassing the SYCE1 gene in one azoospermic man, suggesting SYCE1 is located at rearrangement hotspot [23]. However, many other types of CNVs in SYCE1 which were associated with NOA remain to be elucidated. Also, the association between CNVs with SYCE1 and histopathology still remains unclear.
Herein, we identified two novel CNVs within SYCE1 in two NOA-affected patients. We identified heterozygous deletion within SYCE1 associated with heterozygous LoF variant in SYCE1 in one patient with NOA and a homozygous deletion within SYCE1 in the other patient with meiotic arrest. Hematoxylin and eosin staining (H&E) and immunofluorescence (IF) showed that the spermatogenesis arrested at spermatocyte stage in the two NOA-cases. Thus, our study ascertained CNVs within SYCE1 could result in meiotic arrest and NOA, and provided novel foci for NOA genetic counselling.

Study subjects
In the current study, two Chinese NOA-affected patients were recruited to identify the genetic causal factor of male infertility at our center. The family histories of two patients with NOA were collected. The known causal factors for male infertility were excluded for the two NOA-affected individuals, namely cryptorchidism, hypogonadism, chromosomal abnormalities, genomic AZF micro-deletions, seminal tract obstruction, and other diseases like cancer.

Whole-exome sequencing (WES)
Genomic DNA was extracted from blood samples of two NOA-affected patients using the TIANamp Blood DNA Kit (Tiangen). WES of samples was prepared by VAHTS Universal DNA Library Prep Kit for Illumina V3 (Vazyme) and IDT xGen Exome Research Panel V1.0 (Integrated DNA Technologies). The quantity of sequencing library was assessed by Qubit 3.0 fluorometer (Thermo Fisher Scientific). The quality and size of libraries were measured by 2100 Bioanalyzer High Sensitivity DNA Assay (Agilent Technologies). For next-generation sequencing, the qualified libraries were applied to 2 × 150-bp paired-end sequencing on the Illumina NovaSeq platform (Illumina, San Diego, USA).

In silico analysis
Raw data files were obtained from Novaseq 6000, and then were demultiplexed and converted to fastq format using bcl2fastq software for downstream analysis. Adapters and reads with low quality were trimmed using fastp software. The BAM files were obtained by aligning the sequence reads to the reference (hg19/GRCH37, fasta format) with the use of the SpeedSeq. Additionally, duplicate reads were flagged in the BAM files to prevent downstream variant call errors, sample contamination and swaps using VerifyBamID. Then UnifiedGenotyper tool of GAT was used to call SNVs. The variants were annotated using Annovar software. During the annotation, several public databases such as Clinvar, gnomAD, dbNSFP, etc. were used. Variants with allele frequencies higher than 1% in any public databases (ExAC Browser and gnomAD) were excluded. Because autosomal recessive or X-linked inheritance were assumed for MA, genes with two alleles of potentially deleterious missense mutations (SIFT, PolyPhen-2 and MutationTaster), LoF mutations, or CNVs were kept for further analysis. Moreover, we compared candidate genes with human testisenriched genes in the database (https:// www. prote inatl as. org/) and known pathogenic genes for azoospermia in mice (http:// www. infor matics. jax. org/ mgiho me/ homep ages/).

Sanger sequencing
Validation of SYCE1 SNV in the NOA-affected patient (P6326) and family members was performed by classical Sanger sequencing. Genomic DNA was extracted from peripheral blood using the TIANamp Genomic DNA Blood Kit (TIANGEN, Beijing, China) according to the manufacturer's instructions. The primers were shown as follows: Forward primer: 5′-CAG AGA TGT GGG ATG ACA GAAG-3′; Reverse primer: 5′-AGA AGG TGG AGA GAG GAG ATAC-3′. And the PCR products were bidirectionally sequenced through a 3730xl DNA Analyzer (Applied Biosystems, California, USA).

CNV array
CNV array was performed according to the method as described previously [26]. Briefly, for each blood sample of two patients with NOA and the family members, 250 ng genomic DNA was digested by NspI nuclease for 2 h at 37 °C. Digested DNA and adaptors were ligated by T4 DNA ligase for 3 h at 16 °C. Ligated DNA was amplified, fragmented, end-labeled with biotin and then hybridized to an Affymetrix CytoScan HD Array. Arrays were incubated at 50 °C for 16 h in a Hybridization Oven 645 with rotary motion (60 rpm), followed by washed and stained in a Fluidics Station 450 with protocol "CytoS-canHD_Array_450" and scanned with scanner 3000 7 G controlled by Affymetrix GeneChip Command Console Software (AGCC v4.0.0). Raw data were analyzed by Chromosome Analysis Suite (ChAS) Software v2.1 and copy number was determined by the Affymetrix CytoS-canHD REF model. All microarray experiments were carried out by the CytoScan HD Array Kit and Reagent Kit Bundle (catalogue number: 901835) following the manufacturer's protocol.

Hematoxylin and eosin staining (H&E staining)
The testicular tissues of the two NOA-affected individuals were fixed in 4% paraformaldehyde solution overnight, embedded in paraffin and sectioned at 5 μm thickness. The sections were then stained with Hematoxylin and Eosin solution (catalogue number: ab245880, Abcam, Cambridge, UK) according to standard protocols. The images were captured by phase-contrast microscope (Leica).

Clinical data
Two Chinese patients with infertility participated in this study. The proband (P6326) had a history of male infertility for 5 years. And primary infertility was observed in the other proband (P10377). There was no family history of consanguinity or fertility problems and no chronic diseases in the two NOA-affected patients ( Fig. 1A and B). Neither patient had a history of cryptorchidism, hypogonadism, cancer, drinking, or smoking. Physical examination revealed normal development of penis, epididymis, prostate, scrotum, and vas deferens. Also, there was no varicocele in the two patients with NOA. The volumes of testes in patients (P6326 and P10377) were 15 ml (both sides) and 12 ml (both sides) respectively. Semen analysis revealed normal volume and complete azoospermia on basis of the WHO guidelines (5th edition). Laboratory examination showed that sex hormone levels in both patients were comparable to the reference values (Table 1). Both had 46, XY karyotypes and there were no microdeletions in the Y chromosome.
The probands in families 1 and 2 underwent microsurgical testicular sperm extraction (mTESE) at our center. Histopathological analysis revealed that the Johnsen score of both NOA-affected patients was 5, suggesting MA phenotype in both patients.

Identification of SYCE1 pathogenic variants in the NOA-affected patients
WES assay were performed on the two NOA-affected patients or their family members. After the genetic analyses pipeline aforementioned in the methods, LoF variant (NM_001143763: c.689_690 del:p.F230fs) in SYCE1 was identified using WES and Sanger sequencing ( Fig. 2A and B) in the NOA-affected patient (P6326). The heterozygous frameshift variant (F230fs) was identified in the father ( Fig. 2A and  C). However, the maternal allele appears to be normal ( Fig. 2A and D). It was possible that the proband carried a heterozygous F230fs mutation on the paternal allele and a heterozygous deletion in SYCE1 on the maternal allele. Thus, we employed the WES for CNV analysis in this case according to the protocol as described previously [27,28]. Intriguingly, there  seemed to be CNV in SYCE1 in the proband and the mother (Additional file 1: Fig. 1A-C). Furthermore, CNV array verified that heterozygous deletion (LOH) within SYCE1 (seq[GRCh37] del(10)(10q26.3) chr10:g.135111754_135427143del) was identified in the NOA-affected patient (P6326) and his mother but not in his father ( Fig. 3A-C). Moreover, to evaluate whether the LoF variant (F230fs) are responsible of a reduced protein expression, we generated the mutant SYCE1 (SYCE1-MUT) coding DNA sequence (CDS) cloned downstream of the Flag tag (Flag-SYCE1-MUT). Western blot assay showed a truncated fusion protein, and the expression of mutant SYCE1 was significantly decreased compared with wide type (Flag-SYCE1-WT) (Additional file 1: Fig. 1D). Thus, a paternally inherited frameshift variant led to a truncated SYCE1 protein with reduced expression. And maternally inherited CNV (seq[GRCh37] del(10) (10q26.3)chr10:g.135111754_135427143del) resulted in defect of SYCE1 protein expression in the NOAaffected proband (P6326). For the patient with NOA (P10377), homozygous deletion within SYCE1 (seq[GRCh37] del(10)(10q26.3) chr10:g.135340247_135379115del) was detected via CNV array. Consistent with the autosomal recessive mode of inheritance, the unaffected parents were heterozygous carriers of this same CNV variant (Fig. 3D-F). Collectively, heterozygous LoF SNV associated with heterozygous CNV within SYCE1 were identified in the patient (P6326) and homozygous CNV within SYCE1 was detected in the patient (P10377).

MA Phenotypes in the patients with SYCE1 CNVs
MA phenotypes in the NOA-affected male patients with CNVs within SYCE1 were ascertained by H&E and IF staining. H&E staining results revealed that decreased number of spermatocytes and absence of spermatozoa and spermatids in the testes of the patients with SYCE1 CNVs (P6326 and P10377). However, the number of spermatogonial stem cells (SSCs), differentiated spermatogonia and Sertoli cells at the basement membrane within the seminiferous tubules remained not significantly changed (Fig. 4A-D). IF revealed the expression of DMC1, a marker of double-strand break repair, in the seminiferous tubules, suggesting normal DNA doublestranded break (DSB) repair in the meiosis prophase I in these two patients (P6326 and P10377). However, no signal of PNA (a marker of spermatids and spermatozoa) was detected (Fig. 5A-B). The testicular tissue from OA patients with normal spermatogenesis was also evaluated. And PNA was specifically expressed in acrosome of the haploid germ cells (Fig. 5C). Moreover, SYCP3 and γH2AX foci were expressed in the testis of the NOAaffected patients (Fig. 6A-B). SYCP3 is a marker of components of the axial/lateral element (AE and LE), and γH2AX foci is used to label the DSB, both of which are expressed in preleptotene to zygotene spermatocytes of prophase I. γH2AX can be also used to label the XY body, a specialized meiotic chromatin domain in the nucleus of pachytene spermatocytes. Nevertheless, there was no expression of XY body in seminiferous tubules of these patients with NOA (Fig. 6A-B). And the spermatogenesis was arrested at pachytene stage according to the SYCP3 staining. In contrast, positive expression of SYCP3 and XY body which was indicated by γH2AX staining were observed in testis from the patient with OA (Fig. 6C). Altogether, these results indicated the spermatogenesis arrested at the pachytene stage in the two NOA-affected patients with SYCE1 CNVs.
CNV is the main type of structure variation (SV) caused by genomic rearrangement, which mainly includes deletion and duplication of sub-microscopic genomic segments ranging from 50 bp to several Mb. CNV has been recognized as one of the main genetic factors underlying human diseases. Rearrangement hotspots are the highly homologous regions within segmental duplications (SDs) which could influence rearrangement events. And they are considered antecedents to the formation of CNVs [29]. It was illustrated that 47 hotspots within SYCE1 were detected in 970 Han Chinese men with NOA. However, only one deletion homozygote was identified [23]. Herein, we identified that two novel CNVs within SYCE1 caused meiotic arrest and male infertility. There are no previous reports of CNV (seq[GRCh37] del(10)(10q26.3)chr10:g.135111754_1354  (Table 2).
Previously, two homozygous splice site mutation in the SYCE1 (c.197-2 A > G and c.375-2A > G) were identified in two patients with NOA [12,30]. Furthermore, de Vries et al. reported a nonsense homozygous mutation in the SYCE1 (c.613C > T) in primary ovarian insufficiency (POI) sisters [31]. Thus, deleterious mutation in SYCE1 could result in NOA and POI. Recently, another homozygous mutation (R125G) in SYCE1 was identified in one patient with maturation arrest [32]. Also, Feng et al.reported the same homozygous mutation (F230fs) in SYCE1 in one NOA-affected patient, and the variant was inherited from heterozygous parental carriers [33]. In the present study, for the patient with NOA (P6326), frameshift variant (F230fs) was inherited from the father whilst the CNV is inherited from mother, which was also consistent with the autosomal recessive mode of inheritance. The allele frequency of SYCE1 variant (F230fs) was 1.2 × 10 -5 according to the gnomAD database. And this SYCE1 variant was assessed as deleterious, including PVS1 (For Spermatogenic failure 15, LoF variant of SYCE1 is a known mechanism, this variant is a frameshift variant); PM2 (For recessive disorders, this variant is at extremely low frequency in Exome Sequencing Project,1000 Genomes Project, or Exome Aggregation Consortium); PM3 (For recessive disorders, detected in  Table 2).
The synaptonemal complex (SC) is a highly ordered meiosis-specific scaffold that assembles between homologous chromosomes in the meiosis (Prophase I) and is essential for the formation of meiotic crossovers [34]. And SC structure is conserved between different organisms, including budding yeast, plants, flies, mice, and human. SC at pachytene consists of two lateral elements and the central region, while the central region is comprised of the transverse filaments and the central element (CE). CE proteins have been categorized as synaptic initiation factors (SYCE3, SYCE1, and SIX6OS1) and elongation factors (SYCE2 and TEX12). SYCE1 is the major component of the central element, and it is a meiosisspecific gene located at 10q26 in humans, which has 13 exons encoding a 351-aa protein [35]. Knock-out of Syce1 in mice results in complete loss of tripartite SC structure [36]. It was demonstrated that SYCE1 forms head-ofhead antiparallel dimer via SYCE1 core (aa 25 to 179), and this dimer undergoes conformational change into 1:1 complex upon interaction with SIX6OS1 [35]. The interaction is formed via two interfaces, including SYCE1 core-SIX6OS1N (Interface 1) and SYCE1 177-305 and  [37]. Furthermore, SYCE1 could interact with SYCE3 through C-terminal, which is essential for SC recruitment [38]. In the present study, paternal derived CNV in patient (P6326) leaded to haploinsufficiency in SYCE1. While maternal derived SYCE1 variant (NM_001143763: c.689_690 del:p.F230 fs) resulted in a truncated protein without any effects of SYCE1 core expression. However, this variant blocked the second binding interface with SIX6OS1. And SYCE1-SYCE3 complex could be significantly abolished in this variant, which resulted in severer defects in CE loading. In the NOA-affected patient (P10377), homozygous deletion leaded to no expression of SYCE1 in the meiosis. Thus, the spermatogenesis was completely arrested at pachytene stage in this patient. Altogether, CNVs in SYCE1 caused meiotic arrest and NOA in these two patients.

Conclusions
In conclusion, we identified two novel CNVs within SYCE1 in two idiopathic NOA-affected patients. The meiotic arrest phenotype was ascertained in these two patients via H&E and IF staining. Thus, our study expands the knowledge of variants in SYCE1 and provides a new insight to understand the genetic etiology of